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Nc1nc(/C(=N/O)C(=O)N[C@@H]2C(=O)N3C(C(=O)O)=C(C4CCC(=O)O4)CS[C@H]23)cs1
Reaction #6388
(6R,7R)-7-[2-(2-Aminothiazol-4-yl)-2-(Z)-hydroxyiminoacetamido]-3-[(5RS)-2-oxotetrahydrofuran-5-yl)ceph-3-em-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CCC(Sc1nnn[nH]1)C1=C(C(=O)O)N2C(=O)C(NC(=O)CSC(F)(F)F)[C@H]2SC1
Reaction #55411
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSCC(=O)NC1C(=O)N2C(C(=O)O)=C(C(CCC(N)=O)Sc3nnn[nH]3)CS[C@H]12
Reaction #55414
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(NC(=O)[C@H](O)c2ccccc2)C(=O)N2C(C(=O)O)=C(C(CCC(=O)O)Sc3nnn[nH]3)CS[C@@H]21
Reaction #55420
7β-D-Mandelamido-7α-methoxy-3-[1-(2-carboxyethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1=C(C(CCC(N)=O)Sc2nnn[nH]2)CS[C@@H]2C(N)C(=O)N12
Reaction #55421
7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid t-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C#CCON=C(C(=O)NC1C(=O)N2C(C(=O)O)=C(C(CCO)Sc3nnn[nH]3)CS[C@H]12)c1csc(NC=O)n1
Reaction #55553
7-[2-(2-formamidothiazol-4-yl)-2-propargyloxyiminoacetamido]-3-[1-(2-hydroxyethyl)-1H-tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid
収率 60.4%DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1nc(C(=NOCCOC=O)C(=O)NC2C(=O)N3C(C(=O)O)=C(C(CCO)Sc4nnn[nH]4)CS[C@H]23)cs1
Reaction #55554
7-[2-(2-formamidothiazol-4-yl)-2-(2-formyloxyethoxyimino)acetamido]-3-[1-(2-hydroxyethyl)-1H-tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid
収率 31.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C1=C(C(=O)[O-])N2C(=O)C(NC(=O)C(=NOC(F)F)c3csc(N)n3)[C@H]2SC1)[NH+]1CCCC1
Reaction #62778
7-[2-(2-aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(1-methyl-1-pyrrolidiniomethyl)-3-cephem-4-carboxylate
収率 72.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1Cc2ccccc2C1
Reaction #79288
Ethyl 2,3-dihydo-1H-inden-2-ylacetate
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(Cc2ccccc2)CC1c1nn2c(C3=CCOCC3)ncc2c(=O)[nH]1
Reaction #85993
7
収率 55.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cc(C3=CCOCC3)ccc21
Reaction #91911
title compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnnc1CC(Sc1nnn[nH]1)C1=C(C(=O)O)N2C(=O)C(N)[C@H]2SC1
Reaction #95976
title compound
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(C#N)=C1/CCOC2(CCCC2)C1
Reaction #163404
methyl 2-cyano-2-[(9Z)-6-oxaspiro[4.5]decan-9-ylidene]acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C#N)=C1CCOC2(CCCC2)C1
Reaction #163415
methyl 2-cyano-2-[6-oxaspiro[4.5]decan-9-ylidene]acetate
収率 87.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(C)C1CC(c2ccc(OCc3cc(C)nc4ccccc34)cc2)=NO1
Reaction #183125
DOI: 10.1039/C8SC04228D
COC(=O)C=C1C=CC=C(OCCCN(Cc2cccc(C(F)(F)F)c2Cl)CC(C)c2ccc(Cl)cc2)C1
Reaction #183785
DOI: 10.1039/C8SC04228D
CCC(=CC(=O)OC)c1cc(F)cc(O[Si](C)(C)C(C)(C)C)c1F
Reaction #194447
DOI: 10.1039/C8SC04228D
COC(=O)C=C1C=CC=C(OCCCN(Cc2cccc(C(F)(F)F)c2Cl)CC(C)c2ccccc2OC)C1
Reaction #226885
DOI: 10.1039/C8SC04228D
COC1C=C(C)C(=O)CC(C)(C)C1OC(=O)c1ccc(N)cc1
Reaction #243143
DOI: 10.1039/C8SC04228D
COC(=O)C=C1C=CC=C(OCCCN(Cc2cccc(C(F)(F)F)c2Cl)CC(C)c2ccc(OC)cc2)C1
Reaction #274203
DOI: 10.1039/C8SC04228D
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